rs141686175

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs141686175(A;G)

Make rs141686175(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38872215

Gene

SCN11A

is a	snp
is	mentioned by
dbSNP	rs141686175
dbSNP (classic)	rs141686175
ClinGen	rs141686175
ebi	rs141686175
HLI	rs141686175
Exac	rs141686175
Gnomad	rs141686175
Varsome	rs141686175
LitVar	rs141686175
Map	rs141686175
PheGenI	rs141686175
Biobank	rs141686175
1000 genomes	rs141686175
hgdp	rs141686175
ensembl	rs141686175
geneview	rs141686175
scholar	rs141686175
google	rs141686175
pharmgkb	rs141686175
gwascentral	rs141686175
openSNP	rs141686175
23andMe	rs141686175
SNPshot	rs141686175
SNPdbe	rs141686175
MSV3d	rs141686175
GWAS Ctlg	rs141686175

Max Magnitude

0

ClinVar
Risk	rs141686175(G;G)
Alt	rs141686175(G;G)
Reference	Rs141686175(A;A)
Significance	Pathogenic
Disease	Episodic pain syndrome not specified
Variation	info
Gene	SCN11A
CLNDBN	Episodic pain syndrome, familial, 3 not specified
Reversed	0
HGVS	NC_000003.11:g.38913706A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144934.3, RCV000282888.1,